Home NDC 81033-102 Guaifenesin
Product NDC 81033-102
11-digit product format 810330102
Labeler code 81033
Product ID 81033-102_316ac9e6-8d03-f55a-e063-6294a90a8540
Type HUMAN OTC DRUG
Nonproprietary name Guaifenesin
Dosage form LIQUID
Route ORAL
Labeler KESIN PHARMA CORPORATION
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-11-20
Substance GUAIFENESIN
Active strength 100 mg/5mL
Pharmacologic classes Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings Warnings Do not use if you ever had an allergic reaction to any of the ingredients in this product Ask a doctor before use if you have cough that occurs with too much phlegm (mucus) cough that lasts or is chronic such as occurs with smoking, asthma, chronic, bronchitis, emphysema Stop use and ask a doctor if cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistant headache. These could be signs of a serious condition. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Additional Listing Data#
Finished product Yes
Brand name base Guaifenesin
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GUAIFENESIN 100 mg/5mL
Harmonized Identifiers# Field, Values table Field Values Unii 495W7451VQ Rxcui 310604
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81033-102-05 Guaifenesin 5 mL in 1 CUP, UNIT-DOSE LIQUID 5 7 81033-102-10 Guaifenesin 10 mL in 1 CUP, UNIT-DOSE LIQUID 10 7 81033-102-51 Guaifenesin 50 in 1 CARTON LIQUID 50 7 81033-102-52 Guaifenesin 50 in 1 CARTON LIQUID 50 7 81033-102-16 Guaifenesin 473 mL in 1 BOTTLE LIQUID 473 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81033-102 GUAIFENESIN LIQUID [KESIN PHARMA CORPORATION] 7 Current NDC, 4 package rows 20250331_365c01b7-a197-4876-85fc-42204f787e3a.zip 81033-102 GUAIFENESIN LIQUID [KESIN PHARMA CORPORATION] 1 Current NDC, 1 package rows 20250406_31b8ad0a-3637-03db-e063-6394a90acdc3.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 81033-102-05 81033010205 5 mL in 1 CUP, UNIT-DOSE 5 ml Historical 81033-102-10 81033010210 10 mL in 1 CUP, UNIT-DOSE 10 ml Historical 81033-102-16 81033010216 473 mL in 1 BOTTLE (81033-102-16) 473 ml 2025-04-01 No No Current 81033-102-51 81033010251 50 CUP, UNIT-DOSE in 1 CARTON (81033-102-51) / 5 mL in 1 CUP, UNIT-DOSE (81033-102-05) 2023-11-20 No No Current 81033-102-52 81033010252 50 CUP, UNIT-DOSE in 1 CARTON (81033-102-52) / 10 mL in 1 CUP, UNIT-DOSE (81033-102-10) 2023-11-20 No No Current